没有合适的资源?快使用搜索试试~ 我知道了~
温馨提示
Due to the manifestation of fascinating physical phenomena and materials science, two-dimensional (2D) materials have recently attracted enormous research interest with respect to the fields of electronics and optoelectronics. There have been in-depth investigations of the nonlinear properties with respect to saturable absorption, and many 2D materials show potential application in optical switches for passive pulsed lasers. However, the Eigen band-gap determines the responding wavelength band a
资源推荐
资源详情
资源评论
Band-gap modulation of two-dimensional saturable
absorbers for solid-state lasers
Shuxian Wang,
1
Haohai Yu,
1,2
and Huaijin Zhang
1,3
1
State Key Laboratory of Crystal Materials and Institute of Crystal Materials, Shandong University, Jinan 250100, China
2
e-mail: haohaiyu@sdu.edu.cn
3
e-mail:huaijinzhang@sdu.edu.cn
Received December 24, 2014; revised February 10, 2015; accepted February 12, 2015;
posted February 13, 2015 (Doc. ID 231453); published March 16, 2015
Due to the manifestation of fascinating physical phenomena and materials science, two-dimensional (2D) materi-
als have recently attracted enormous research interest with respect to the fields of electronics and optoelectronics.
There have been in-depth investigations of the nonlinear properties with respect to saturable absorption, and many
2D materials show potential application in optical switches for passive pulsed lasers. However, the Eigen band-gap
determines the responding wavelength band and constrains the applications. In this paper, based on band-gap
engineering, some different types of 2D broadband saturable absorbers are reviewed in detail, including molyb-
denum disulfide MoS
2
, vanadium dioxide VO
2
, graphene, and the Bi
2
Se
3
topological insulator. The results
suggest that the band-gap modification should play important roles in 2D broadband saturable materials and
can provide some inspiration for the exploration and design of 2D nanodevices. © 2015 Chinese Laser Press
OCIS codes: (140.0140) Lasers and laser optics; (140.3540) Lasers, Q-switched; (140.3380) Laser materials;
(140.3538) Lasers, pulsed.
http://dx.doi.org/10.1364/PRJ.3.000A10
1. INTRODUCTION
Lasers, since first demonstrated by a ruby crystal in 1960 [1],
have shown tremendous progress so far. On account of the
advantages of large pulse energy, short pulse duration, and
high peak power, pulse lasers, including mode-locking and
Q-switching, receive more widespread attention [
2,3]. Pulsed
lasers with the pulse width from nanosecond to subpicosec-
ond scales play a key role in the industrial machining, remote
sensing, and military defense areas [
4]. Ultrashort femtosec-
ond lasers have significant applications in the fields of the
in-situ detection, complex reaction dynamics, medical survey,
and telecommunication [
3]. Passive pulse modulation could
be operated with compact and cost-effective structures, such
that it has become an influential research direction in the laser
field. Taking advantage of saturable absorption of saturable
absorbers, that is part of the third-order nonlinear properties,
passive pulse modulation in the Q-switched or mode-locking
lasers could be easily implemented. Traditional saturable
absorbers, such as ion-doped crystals (Cr:YAG, Cr:ZnSe, V:
YAG, and so on) [
5–7], GaAs [8], and color-center crystals
(for example F
2
:LiF) [9], are wavelength-sensitive and are
only applied in their respective corresponding wavelength
bands. Although the commercial semiconductor saturable
absorber mirrors (SESAMs) could be fabricated for the
specific wavelength from 0.4 to 2.5 μm by using different
semiconductor material systems [
2,10], the relatively complex
structural design may increase the product cost and the diffi-
culty of preparation. In addition, the quasi-phase-matching
technique in optical superlattice, which is feasible for a wide
wavelength range as long as it is in the transparent spectral
region of the optical superlattice material, is also a promising
method to obtain passive mode-locking lasers [
11–13].
Nevertheless, this technique requires the high-efficiency
generation of second-harmonic generation and elaborate
design of the resonant cavity and the second-harmonic
crystal. Therefore, the development of low-cost and robust
broadband saturable absorbers is still an intense focus of
research nowadays [
2].
Graphene, as the representative of the two-dimensional
(2D) materials, since found by K. Geim and K. S. Novoselov,
has profoundly promoted and broadened the research areas
of 2D materials in the fields of electronics and optoelectronics
due to an abundance of fantastic physics [
14–23]. With in-
depth studies, many other novel 2D materials are discovered
and are brought into people’s horizons, such as transition
metal dichalcogenides (TMDCs) (typically MoS
2
, MoSe
2
,
WS
2
, and so on) [16,17,19,24,25], transition metal oxides
(for instance MoO
3
and TiO
2
)[17,24,26], topological insula-
tors (Bi
2
Se
3
,Bi
2
Te
3
, and Sb
2
Te
3
)[16,17,24,27], as well as sil-
icone [
28], germanane [16,28], black phosphorus [29,30], and
other graphene analogues (typically h-BN) [
19,24]. For the ma-
jor 2D materials, the layered structure results in the strong in-
plane coupling and the weak van der Waals coupling between
layers. Therefore monolayer or few-layer 2D perfect samples
could be easily fabricated by mechanical exfoliation or chemi-
cal exfoliation [
18,31]. In addition, aiming at the growth habits
and atomic arrangements for different 2D materials, many
more efforts are made to explore the economical and practical
growth methods, such as chemical vapor deposition, and epi-
taxial growth on adaptive substrates [
21,25]. The layered 2D
materials exhibit numerous exotic physical, chemical, and
mechanical properties such that they are rapidly developed.
Many potential functional applications in terms of 2D
materials in some aspects will be realized in the near future,
A10 Photon. Res. / Vol. 3, No. 2 / April 2015 Wang et al.
2327-9125/15/020A10-11 © 2015 Chinese Laser Press
including optical modulators, photodetectors, logic transis-
tors, high-frequency transistors, energy storage, and sensor
devices [
16–18,24,31].
Most 2D semiconductor materials show a simple two en-
ergy band structure of the conduction band and the valence
band. Light that is of higher energy than the gap energy can
excite carriers from the valance band to the conduction band.
If the excitation has stronger intensity, all possible initial
states are depleted and the final states are partially occupied
in accordance with the Pauli blocking effect such that the ab-
sorption will be saturated [
2]. Thus the 2D semiconductor
materials give some opportunities for the fabrication of
cost-effective and flexible broadband saturable absorbers,
and some 2D materials have realized this goal [
4,32–34]. Satu-
rable absorption is the modulation of nonlinear absorption.
However, the bandgap of a semiconductor determines the
responding wavelength and every semiconductor has its spe-
cialized bandgap. Based on the photoelectric effect, the semi-
conductors materials with a narrow bandgap have broad
responding wavelength bands. Therefore, besides the narrow
bandgap, for 2D materials such as graphene, the modulation
of the bandgap should be important, especially for the materi-
als with large bandgaps such as MoS
2
[13,35]. In this review,
what is discussed will mainly concentrate on the state-of-the-
art research exploration and development about the saturable
absorbers for several 2D materials. The content consists of the
band-gap modification by impurity of MoS
2
, band-gap modu-
lation by phase transition of VO
2
, and broadband modulation
by inherent bandgaps for graphene and Bi
2
Se
3
topological
insulator. This work can show some guiding designing func-
tions for the investigation of other 2D layered optoelectronic
materials.
2. BAND-GAP ENGINEERING FOR MoS
2
Layered MoS
2
, a typical representative of the layered TMDCs
family, is composed of the sandwiches combined by van der
Waals interactions, and each sandwich consists of covalently
bound S–Mo–S trilayers with two hexagonal layers of S atoms
and an intermediate hexagonal plane of Mo atoms [
17,25,36–
38]. The monolayer MoS
2
has a direct band-gap at the K point
of the Brillouin zone with a gap of 1.8 eV (0.7 μm), and the bulk
MoS
2
is of an indirect band-gap between the Γ point (valence
band) and K point (conduction band) of the Brillouin zone
with a gap of ranging from 0.86 eV (1.4 μm) to 1.29 eV
(1.0 μm) [
39–44]. Besides the change of thickness, the
bandgap of MoS
2
was also modified by the other engineering
technologies, such as the external electric field and the exter-
nal strain [
45–48]. Atomic-layered MoS
2
exhibits intriguing
physical properties distinct from its bulk state, for example,
the dramatical increasing of luminescence quantum efficiency
for MoS
2
from the bulk state to single layer. Therefore, layered
MoS
2
attracts more interest in the fabrication of ultrathin and
flexible nanoelectronic devices [
16,25], and was brought into
various research fields, such as lubrication, hydrodesulfuriza-
tion catalysis, supercapacitors, and field-effect transistors
[
36–38,49].
Monolayer MoS
2
has been proven with strong optical
response, such as enhanced photon absorption and large
photocurrent caused by van Hove singularities or band nest-
ing [
50,51]. In 2012, using the spatially and temporally resolved
pump-probe technique with a 390 nm pump source and a
660 nm probe source, R. Wang et al. measured and discussed
the ultrafast carrier dynamics of atomically thin MoS
2
[52].
One year later, more nonlinear investigations were carried
out [
53–55], and it is significant that ultrafast saturable absorp-
tion of MoS
2
nanosheets was demonstrated around 800 nm by
K. P. Wang et al. [
56].
Most of the studies were in pursuit of the high-quality lay-
ered MoS
2
samples in order to obtain remarkable electronic
and optical properties [
37–39]; however, the generation of
defects, which deviate from a perfect crystal structure, was
inevitable in the preparation of MoS
2
samples. The probable
defects could localize electronic states and change the energy
level, leading to some fantastic physical phenomena, such as
the Mott transition and Anderson localization [
57].
Recently, S. X. Wang et al. systematically analyzed the
band-gap change of multilayer MoS
2
in a theoretical analysis
with the ratio R between Mo and S atoms slightly deviating
from 1:2 [
34]. The first-principle theoretical calculations were
performed by using the plane-wave basis Vienna ab initio sim-
ulation package [
58,59], and the atomic arrangement of MoS
2
was the universal AB stacking 2H − MoS
2
. As shown in Fig. 1,
the bandgap is about 1.08 eV (1.2 μm) for multilayered MoS
2
with the stoichiometric ratio, which corresponds well to the
previous calculated value for bulk MoS
2
[40]. The other results
with different R values are displayed in Fig.
2. When R is larger
than 2.09, MoS
2
exhibits metallic character, and the genera-
tion of saturable absorption requiring suitable patterns or dis-
tances between the metal units becomes difficult. When the R
is located in the range 1.89–2 and 2–2.09, few-layered MoS
2
showed an indirect semiconductor property and its energy
gap is 0.08 eV (15.5 μm), 0.23 eV (5.4 μm), 0.48 eV
(2.6 μm), 0.63 eV (2.0 μm), and 0.26 eV (4.7 μm) for the R with
a value of 2.09, 2.04, 1.97, 1.94, and 1.89, respectively. Thus, it
can be concluded that the band-gap of MoS
2
would be reduced
by the introduction of some Mo or S defects in a suitable
range. The smaller band-gap means the broadband saturable
absorption of defective MoS
2
becomes possible.
Then the MoS
2
samples were fabricated by the pulse laser
deposition (PLD) method, which is an efficient technique to
produce the S imperfections for MoS
2
samples, since low-
mass S is evaporated more easily than high-mass Mo [
60].
The R lies in the range 1.89–1.97 moving from the center to
the edge of the sample surveyed by X-ray photoelectron spec-
trometry. As demonstrated in Fig.
3, the measured absorbance
of the MoS
2
sample decreases with an increase of wavelength
[
34]. For the R with the value of 1.89, the energy gap for
MoS
2
samples is only 0.26 eV, corresponding to a wavelength
of 4.7 μm. In contrast to the absorption range of standard
Fig. 1. Brillouin zone (left) and calculated band structure (blue lines,
right) of bulk MoS
2
with stoichiometric ratio. Selected from Ref. [34].
Wang et al. Vol. 3, No. 2 / April 2015 / Photon. Res. A11
剩余10页未读,继续阅读
资源评论
weixin_38723027
- 粉丝: 9
- 资源: 987
上传资源 快速赚钱
- 我的内容管理 展开
- 我的资源 快来上传第一个资源
- 我的收益 登录查看自己的收益
- 我的积分 登录查看自己的积分
- 我的C币 登录后查看C币余额
- 我的收藏
- 我的下载
- 下载帮助
最新资源
资源上传下载、课程学习等过程中有任何疑问或建议,欢迎提出宝贵意见哦~我们会及时处理!
点击此处反馈
安全验证
文档复制为VIP权益,开通VIP直接复制
信息提交成功